Comprehensive assessment of actionable genomic alterations in primary colorectal carcinoma using targeted next-generation sequencing
Autor: | Yi-Hua Jan, Kien Thiam Tan, Shu-Jen Chen, Timothy Tak Chun Yip, Cu tai Lu, Alfred King-yin Lam |
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Rok vydání: | 2022 |
Předmět: |
Proto-Oncogene Proteins B-raf
Cancer Research Class I Phosphatidylinositol 3-Kinases High-Throughput Nucleotide Sequencing Drugs Investigational Genomics Calcium Hydroxide Proto-Oncogene Proteins p21(ras) Oncology Mutation Humans Microsatellite Instability Zinc Oxide Colorectal Neoplasms Immune Checkpoint Inhibitors |
Zdroj: | British journal of cancer. 127(7) |
ISSN: | 1532-1827 |
Popis: | Background The clinical utility of comprehensive genomic profiling (CGP) for guiding treatment has gradually become the standard-of-care procedure for colorectal carcinoma (CRC). Here, we comprehensively assess emerging targeted therapy biomarkers using CGP in primary CRC. Methods A total of 575 primary CRCs were sequenced by ACTOnco® assay for genomic alterations, tumour mutational burden (TMB), and microsatellite instability (MSI). Results Eighteen percent of patients were detected as MSI-High (MSI-H), and the remaining cases were classified as microsatellite stable (MSS). Driver mutation prevalence in MSS CRCs were APC (74%), TP53 (67%), KRAS (47%), PIK3CA (21%) and BRAF (13%). The median TMBs for MSI-H and MSS patients were 37.8 mutations per mega base (mut/Mb) and 3.9 mut/Mb, respectively. Forty-seven percent of MSI-H CRC harboured at least one loss-of-function mutations in genes that may hamper immune checkpoint blockade. Among MSS RAS/RAF wild-type CRCs, 59% had at least one actionable mutation that may compromise the efficacy of anti-EGFR therapy. For late-stage CRC, 51% of patients are eligible for standard care actionability and the remaining 49% could be enrolled in clinical trials with investigational drugs. Conclusions This study highlights the essential role of CGP for identifying rational targeted therapy options in CRC. |
Databáze: | OpenAIRE |
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